α-synuclein gene haplotypes are associated with Parkinson’s disease

By de Silva R.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1847-1851

Oxford University Press

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Analysis of the α-synuclein gene dosage variation associated with autosomal dominant form of Parkinson’s disease

By Semenova E.   Shadrina M.   Slominsky P.   Illarioshkin S.   Bagyeva G.   Karabanov A.   Ivanova-Smolenskaia I.   Limborska S.  

Russian Journal of Genetics, Vol. 45, Iss. 4, 2009-04 ,pp. : 504-506

MAIK Nauka/Interperiodica

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Sequencing of the α-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations

By Lincoln S.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 751-753

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Impaired dopamine storage resulting from α - synuclein mutations may contribute to the pathogenesis of Parkinson's disease

By Lotharius J.   Brundin P.  

Human Molecular Genetics, Vol. 11, Iss. 20, 2002-10 ,pp. : 2395-2407

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Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson's disease

By Mizuta Ikuko   Satake Wataru   Nakabayashi Yuko   Ito Chiyomi   Suzuki Satoko   Momose Yoshio   Nagai Yoshitaka   Oka Akira   Inoko Hidetoshi   Fukae Jiro   Saito Yuko   Sawabe Motoji   Murayama Shigeo   Yamamoto Mitsutoshi   Hattori Nobutaka   Murata Miho   Toda Tatsushi  

Human Molecular Genetics, Vol. 15, Iss. 7, 2006-04 ,pp. : 1151-1158

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